Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Brachial plexus lesion
Frequent (30-79%)
Glutaric aciduria, type 2
Very rare (1-4%)
Neuralgic amyotrophy
Frequent (30-79%)
Langer-Giedion syndrome
Multiple lentigines syndrome
Frequent (30-79%)
Emery-Dreifuss muscular dystrophy
Frequent (30-79%)
Scapuloperoneal muscular dystrophy
Frequent (30-79%)
Scapuloperoneal spinal muscular atrophy
Klein-Waardenberg's syndrome
WSS - Wrinkly skin syndrome
Autosomal recessive centronuclear myopathy
Occasional (5-29%)
Trichorhinophalangeal dysplasia type I
Eosinophilic myositis
Facioscapulohumeral muscular dystrophy
Very frequent (80-99%)
Andersen Tawil syndrome
MEMSA - myoclonic epilepsy myopathy sensory ataxia
Occasional (5-29%)
3-M syndrome
Congenital scoliosis with unilateral unsegmented bar
MPRM - myopathy, proximal, with early respiratory muscle involvement
Frequent (30-79%)
Hereditary inclusion body myopathy
Occasional (5-29%)
Lower motor neuron degeneration with Paget-like bone disease
Mitochondrial membrane protein associated neurodegeneration
Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D)
Frequent (30-79%)
Autosomal recessive limb girdle muscular dystrophy type 2A
Frequent (30-79%)
Autoimmune necrotizing myopathy
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 17211005
- UMLS CUI
- C0240953
- Fully Specified Name
- Winged scapula (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.